Genome Complexity Browser: Visualization and quantification of genome variability

Alexander Manolov, Dmitry Konanov, Dmitry Fedorov, Ivan Osmolovsky, Rinat Vereshchagin and Elena Ilina

PLOS Computational Biology, 2020, vol. 16, issue 10, 1-20

Abstract: Comparative genomics studies may be used to acquire new knowledge regarding genome architecture, which defines the rules for combining sets of genes in the genome of living organisms. Hundreds of thousands of prokaryotic genomes have been sequenced and assembled. However, computational tools capable of simultaneously comparing large numbers of genomes are lacking. We developed the Genome Complexity Browser, a tool that allows the visualization of gene contexts, in a graph-based format, and the quantification of variability for different segments of a genome. The graph-based visualization allows the inspection of changes in gene contents and neighborhoods across hundreds of genomes, simultaneously, which may facilitate the identification of conserved and variable segments of operons or the estimation of the overall variability associated with a particular genome locus. We introduced a measure called complexity, to quantify genome variability. Intraspecies and interspecies comparisons revealed that regions with high complexity values tended to be located in areas that are conserved across different strains and species.Author summary: The comparison of genomes among different bacteria and archaea species has revealed that many species frequently exchange genes. Occasionally, such horizontal gene transfer events result in the acquisition of pathogenic properties or antibiotic resistance in the recipient organism. Previously, the probabilities of gene insertions were found to vary, with unequal distributions along a chromosome. At some loci, referred to as hotspots, changes occur with much higher frequencies compared with other regions of the chromosome. We developed a computational method and a software tool, called Genome Complexity Browser, that allows the identification of genome variability hotspots and the visualization of changes. We compared the localization of various hotspots and revealed that some demonstrate conserved localizations, even across species, whereas others are transient. Our tool allows users to visually inspect the patterns of gene changes in graph-based format, which presents the visualization in a format that is both compact and informative.

Date: 2020
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Persistent link: https://EconPapers.repec.org/RePEc:plo:pcbi00:1008222

DOI: 10.1371/journal.pcbi.1008222

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